Try to answer these Organic Chemistry MCQs and check your understanding of the Organic Chemistry subject. Scroll down and let's begin!
A. Sp2
B. Lone pair
C. Sp3
D. Sp
A. The boiling points
B. With single bonds
C. A double bond between carbon atoms
D. Octane
A. Ketones
B. Carbon bonded to three alkyl groups
C. Skunky or bad smelling odors
D. Carbon bonded to two alkyl groups
A. 4
B. 3
C. 2
D. 1
A. Mirror-image isomers of a molecule
B. Hydrophobic, non polar, and good source of stored energy
C. Cis - trans isomers
D. May not be equally effective
A. Contain an -OH group
B. Are mirror images
C. Differ in the arrangement of their molecules about a double bond
D. Contain a carboxyl group
E. Are isomers that differ in the covalent partnerships between their atoms
A. C–C
B. C–N
C. C–Cl
D. C–F
E. C–O
A. The behavior of any molecule containing a carbon atom was fundamentally the same
B. Under certain circumstances the theory of vitalism was valid
C. A large variety of organic compounds could be spontaneously synthesized from components in Earth's primitive atmosphere
D. Lightning discharges could produce the molecules previously presumed to have originated in volcanic outgassings
E. Urea could be synthesized from entirely naturally occurring salts
A. Contract; heated
B. Expand; cooled
C. Expand; heated
D. Keep the same volume when heated or cooled
A. A primary alcohol
B. A secondary alcohol
C. A tertiary alcohol
D. A phenol
E. An enol
A. -O -
B. -COO -
C. -NH4 -
D. -C=O
A. 227
B. 123
C. 223
D. 226
A. Three σ bonds
B. Three π bonds
C. Two σ bonds and one π bond
D. One σ bond and two π bonds
A. Has two fewer carbon atoms than the corresponding alkane
B. Has two fewer hydrogen atoms than the corresponding alkane
C. Contains - CH3 groups joined by single bonds
D. Always contains a three carbon ring
A. Sulfhydryl group (-SH)
B. Take place in nuclear reactors
C. Are always fusion reactions
D. Never produce radioactive by-products
A. Lack of H atoms
B. Orbital
C. Bohr orbit
D. Atomic Orbit
A. Three
B. Two
C. Four
D. Five
A. Positive
B. Negative
C. Zero
D. Neutral
A. Less vigorous
B. More dilute
C. More saline
D. Stronger
A. 26; 58.
B. 58; 26.
C. 26; 32.
D. 32; 26.
A. S
B. P
C. Sp
D. Sp2
E. Sp3
A. Carbon readily forms ionic bonds
B. Carbon's first electron shell holds 4 electrons
C. A carbon atom can complete its valence shell by forming four covalent bonds
D. The bond angle between each bond is 90°, forming an arrangement like the points on a compass
E. Carbon has a total of 4 electrons
A. The chemical versatility of carbon atoms
B. The variety of rare elements in organic molecules
C. The diverse bonding patterns of nitrogen
D. Their interaction with water
A. The number of carbon atoms in the longest chain
B. Functional group
C. The type of carbon—carbon bonds
D. Reactivity
A. Amino
B. Carboxyl
C. Carboxyl and amino groups
D. Carbon
A. Form enantiomers.
B. Carboxyl and amino groups
C. Carboxyl
D. Hydroxyl
A. Can form a variety of carbon skeletons and host functional groups
B. Organic molecules can be synthesized abiotically under conditions that may have existed on early Earth
C. Simple organic compounds, amino acids, and hydrocarbons
D. The presence or absence of double bonds between the carbon atom and other atoms
A. Water (H2O)
B. Methyl group (-CH3)
C. Carbon
D. COOH and -NH2
A. Acid, amino
B. Called hydrocarbons
C. Lack of H atoms
D. Water (H2O)
A. They contribute to the molecular shape of a molecule and its unique properties
B. Abiotic compounds cycled through the apparatus and were sampled for organic compounds
C. The same molecular formula but different covalent arrangements of heir carbon skeletons
D. A carbon atom can complete its valence shell by forming four covalent bonds
A. Are isomers in which one of the molecules contains an amino group and the other contains a phosphate group
B. Differ in their molecular formulas
C. Differ in the arrangement of their atoms about a double bond
D. Are isomers that differ in the covalent partnerships between their atoms
E. Are mirror images
A. Chemical reactions
B. Chemical reproduction
C. Chemical bonding
D. None of these